Gilead Sciences has won European approval for Yescarta (axicabtagene ciloleucel) for the treatment of certain adults with different kinds of large B-cell lymphoma (LBCL).
Following on from US Food and Drug Administration approval in April, the decision paves the way for a new use of the CAR T-cell therapy in Europe, in the second-line setting.
The outcome will enable Gilead, through its subsidiary Kite Pharma, to continue growing revenues of the therapy, with last year’s sales coming in at $695 million globally.
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